Abstract

Viral Nervous Necrosis (VNN) causes high mortality and reduced growth in farmed European sea bass (Dicentrarchus labrax) in the Mediterranean. In the current studies, we tested a novel Pichia-produced virus-like particle (VLP) vaccine against VNN in European sea bass, caused by the betanodavirus “Red-Spotted Grouper Nervous Necrosis Virus” (RGNNV). European sea bass were immunized with a VLP-based vaccine formulated with different concentrations of antigen and with or without adjuvant. Antibody response was evaluated by ELISA and serum neutralization. The efficacy of these VLP-vaccine formulations was evaluated by an intramuscular challenge with RGNNV at different time points (1, 2 and 10 months post-vaccination) and both dead and surviving fish were sampled to evaluate the level of viable virus in the brain. The VLP-based vaccines induced an effective protective immunity against experimental infection at 2 months post-vaccination, and even to some degree at 10 months post-vaccination. Furthermore, the vaccine formulations triggered a dose-dependent response in neutralizing antibodies. Serologic response and clinical efficacy, measured as relative percent survival (RPS), seem to be correlated with the administered dose, although for the individual fish, a high titer of neutralizing antibodies prior to challenge was not always enough to protect against disease. The efficacy of the VLP vaccine could not be improved by formulation with a water-in-oil (W/O) adjuvant. The developed RGNNV-VLPs show a promising effect as a vaccine candidate, even without adjuvant, to protect sea bass against disease caused by RGNNV. However, detection of virus in vaccinated survivors means that it cannot be ruled out that survivors can transmit the virus.

Highlights

  • Viral nervous necrosis (VNN), or viral encephalo- and retinopathy (VER), is a viral disease of many marine and freshwater fish, including European sea bass (Dicentrarchus labrax), causing an infection of the central nervous system with spiraling swimming pattern, loss of buoyancy control and darkening of the skin being some of the most evident clinical manifestations [1,2,3,4]

  • The Western blot confirmed the same size of the virus-like particle (VLP) and Red-Spotted Grouper Nervous Necrosis Virus” (RGNNV) virus capsid proteins (Figure 3) as well as antigenic similarity in terms of the polyclonal rabbit-anti-nodavirus antibody binding to both

  • We present an RGNNV VLP able to induce a dose-dependent response of neutralizing antibodies in European sea bass

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Summary

Introduction

Viral nervous necrosis (VNN), or viral encephalo- and retinopathy (VER), is a viral disease of many marine and freshwater fish, including European sea bass (Dicentrarchus labrax), causing an infection of the central nervous system with spiraling swimming pattern, loss of buoyancy control and darkening of the skin being some of the most evident clinical manifestations [1,2,3,4]. RNA1 (3.1 kb) encodes the RNA-dependent RNA polymerase 100 kDa) involved in the viral replication and with a + 1 shift in reading frame a subgenomic RNA3 (0.4 kb) is translated, encoding for protein B2 which suppress cellular RNA interference [5]. RNA 2 (1.4 kb) encodes the capsid protein The p-domain determines the host specificity of the virus and harbors the variable T4 region used to classify the Betanodavirus into four species: red-spotted grouper (RG) nervous necrosis virus (NNV), striped jack-(SJ)NNV, tiger puffer-(TP)NNV and barfin flounder (BF)NNV. The species can re-assort the two RNA segments, giving rise to re-assortant strains with, e.g., RNA1 from RGNNV and RNA2 from SJNNV (RG/SJNNV) [7]. The four species are antigenically different and have been divided into three serotypes; RGNNV belong to serotype C, while SJNNV and TPNNV are serotypes A and B, respectively. BFNNV has been classified both as serotype C [8,9] and B [10]

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